CymitQuimica logo

CAS 850567-34-9

:

B-[3-[(2-Thiazolylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(2-Thiazolylamino)carbonyl]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and other Lewis bases. This compound features a phenyl ring substituted with a thiazole moiety, which contributes to its biological activity and potential applications in medicinal chemistry. The thiazole ring is a five-membered heterocycle containing sulfur and nitrogen, enhancing the compound's reactivity and interaction with biological targets. Boronic acids are often utilized in drug discovery due to their role in the development of protease inhibitors and their ability to modulate biological pathways. The presence of the carbonyl group linked to the thiazole further suggests potential for hydrogen bonding and interactions with biomolecules. Overall, B-[3-[(2-Thiazolylamino)carbonyl]phenyl]boronic acid exemplifies the versatility of boronic acids in chemical synthesis and their significance in pharmaceutical applications.
Formula:C10H9BN2O3S
InChI:InChI=1S/C10H9BN2O3S/c14-9(13-10-12-4-5-17-10)7-2-1-3-8(6-7)11(15)16/h1-6,15-16H,(H,12,13,14)
InChI key:InChIKey=ORXREXRVDUFDBS-UHFFFAOYSA-N
SMILES:C(NC1=NC=CS1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • Boronic acid, B-[3-[(2-thiazolylamino)carbonyl]phenyl]-
  • [3-[(1,3-Thiazol-2-yl)carbamoyl]phenyl]boronic acid
  • B-[3-[(2-Thiazolylamino)carbonyl]phenyl]boronic acid
  • [3-(Thiazol-2-ylcarbamoyl)phenyl]boronic acid
  • Boronic acid, [3-[(2-thiazolylamino)carbonyl]phenyl]-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.